University of Iowa 3 credits PHAR
Focus on determinants in protein small molecule binding, particularly involving pharmaceutically relevant enzymes and receptors; how modern structure-based drug discovery is greatly aided by ability to employ protein structures in discovery and design of certain classes of drugs; structural approaches for predicting and improving drug affinity and selectivity, which have made a lasting impact across a number of diseases; important contemporary topics include in-depth lectures on fragment based drug discovery (FBDD), use and pitfalls of in silico docking and other screening methods, and emergence of covalent drugs. Requirements: introductory course in biochemistry.
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